OMC Medical Limited | Regulatory Affairs Specialist

Role Description This is a full-time on-site role for a Regulatory Affairs Associate at OMC Medical Limited. The Regulatory Affairs Associate will be responsible for handling regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, preparing regulatory submissions, and managing overall regulatory affairs for medical...

About the RoleThis is a full-time on-site position for a Regulatory Affairs Associate at OMC Medical Limited. The successful candidate will be responsible for handling regulatory documentation, ensuring regulatory compliance with medical devices and cosmetics regulations, and managing overall regulatory affairs.Key ResponsibilitiesPreparing and reviewing...

Job Title: Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in Bengaluru. As a key member of our organization, you will play a vital role in ensuring compliance with regulatory requirements and driving the success of our medical device testing business.About Us:BioTalent Search Private Limited is a...

Apsida Life Science are looking for a Regulatory Affairs Specialist for a long term project.Immediate start!!!You will need to Provide regulatory advice, verify strategic approaches and timelines, and align zone strategies with Affiliate Regulatory Affairs teams.Apply knowledge of regulatory requirements in Vietnam, Philippines, Thailand, Malaysia, Singapore...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Biocon in US/Canada Market. This role is an exciting opportunity for individuals with experience in formulation regulatory affairs.Key ResponsibilitiesPrepare, review and submit ANDA/ANDS in the US Market, including modules.Contribute to life cycle management for...

**Job Description**: You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping...

Apsida Life Science are looking for a Regulatory Affairs Specialist for a long term project. Immediate start!!! You will need to Provide regulatory advice, verify strategic approaches and timelines, and align zone strategies with Affiliate Regulatory Affairs teams. Apply knowledge of regulatory requirements in Vietnam, Philippines, Thailand, Malaysia,...

Apsida Life Science are looking for a Regulatory Affairs Specialist for a long term project. Immediate start!!! You will need to Provide regulatory advice, verify strategic approaches and timelines, and align zone strategies with Affiliate Regulatory Affairs teams. Apply knowledge of regulatory requirements in Vietnam, Philippines, Thailand, Malaysia,...

Apsida Life Science are looking for a Regulatory Affairs Specialist for a long term project.Immediate start!!!You will need to Provide regulatory advice, verify strategic approaches and timelines, and align zone strategies with Affiliate Regulatory Affairs teams.Apply knowledge of regulatory requirements in Vietnam, Philippines, Thailand, Malaysia, Singapore...

Apsida Life Science is seeking a Regulatory Affairs Specialist for a long-term project in the Asia-Pacific region. The ideal candidate will have expertise in regulatory requirements for Vietnam, Philippines, Thailand, Malaysia, Singapore, and other ROW countries.The role involves providing strategic guidance on regulatory compliance, collaborating with...

Clinical Affairs ManagerJoin the Future of HealthcareTC4A, a pioneer in democratizing healthcare innovations, is revolutionizing diagnostics with LightAI. We are seeking talented individuals to join our office in Noida and address one of healthcare’s biggest challenges, the overuse of antibiotics that leads to drug-resistant infections and costs billions...

Clinical Affairs Manager Join the Future of Healthcare TC4A, a pioneer in democratizing healthcare innovations, is revolutionizing diagnostics with LightAI. We are seeking talented individuals to join our office in Noida and address one of healthcare’s biggest challenges, the overuse of antibiotics that leads to drug-resistant infections and costs...

About Qure.AI: Qure.AI is the world's fastest-growing medical AI company, boasting an impressive 18 FDA and 62 CE marking clearances to date. We develop cutting-edge solutions that significantly enhance patient outcomes across various care domains, including lung cancer, tuberculosis, and stroke. Our innovative technologies have positively impacted...

About Qure.AI: Qure.AI is the world's fastest-growing medical AI company, boasting an impressive 18 FDA and 62 CE marking clearances to date. We develop cutting-edge solutions that significantly enhance patient outcomes across various care domains, including lung cancer, tuberculosis, and stroke. Our innovative technologies have positively impacted...

We are hiring for our rapidly growing client in the biotech IVD manufacturing business, based in Bengaluru.Job Title: Regulatory Affairs AssociateLocation: BengaluruEducation:Bachelor’s or Master’s degree in Engineering, Biomedical Sciences, or a related discipline.Certifications in regulatory compliance or quality systems (e.g., RAC, CQE) are a...

The Regulatory Manager will be responsible for overseeing and ensuring that all food compliance mandates related to FSSAI and AYUSH formulation guidelines are strictly adhered to. This includes managing compliance for Zeon's domestic product range, which covers Proprietary Foods, Nutraceuticals, Health Supplements, Food for Special Dietary Users (FSDU),...

We are hiring for our rapidly growing client in the biotech IVD manufacturing business, based in Bengaluru. Job Title: Regulatory Affairs Associate Location: Bengaluru Education: Bachelor’s or Master’s degree in Engineering, Biomedical Sciences, or a related discipline. Certifications in regulatory compliance or quality systems (e.g., RAC, CQE) are a...

We are hiring for our rapidly growing client in the biotech IVD manufacturing business, based in Bengaluru. Job Title: Regulatory Affairs Associate Location: Bengaluru Education: Bachelor’s or Master’s degree in Engineering, Biomedical Sciences, or a related discipline. Certifications in regulatory compliance or quality systems (e.g., RAC, CQE) are a...

Job Description:As a Medical Information Quality Specialist at ARDEM Data Services, you will play a critical role in ensuring the accuracy and quality of medical documents. This position is ideal for individuals with a strong background in life sciences and a keen eye for detail.Key Responsibilities:Document Review: Conduct thorough reviews of various...

About Medisal Pharma As a proud United Arab Emirates company based in Abu Dhabi, Medisal Pharma is dedicated to excellence in manufacturing high-quality pharmaceutical products to enhance global health by developing and delivering high-quality, affordable medicines. With a strong emphasis on innovation, research, and excellence, we aim to make a...